小鼠巨噬细胞质膜抗原F4/80的历史征程

IF 3.1 3区 医学 Q3 CELL BIOLOGY
Siamon Gordon, Annabell Roberti, Simon Yona, Hsi-Hsien Lin
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引用次数: 0

摘要

随着F4/80抗原被发现近半个世纪,作为小鼠组织巨噬细胞的分化标记物的广泛使用,继续在实验细胞免疫学内外提出问题。它作为7跨膜G蛋白偶联受体的结构开启了质膜受体多样化家族的发现。本综述将追踪F4/80(也称为Emr1)表达研究的里程碑,其作为单核吞噬细胞系统形成标志物的价值及其在眼前房外周免疫耐受模型中的功能。人类EMR1与灵长类动物限制性髓系机械受体EMR2密切相关,具有新的自催化激活机制。我们描述了它们与E组粘附GPCR亚家族结构相关成员的关系,以及它们通过局部质膜细胞相互作用对体内稳态系统的贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
F4/80, the plasma membrane antigen of mouse macrophages, an historic journey.

As its discovery nears a half century, the widespread use of F4/80 antigen as a differentiation marker of tissue macrophages of the mouse, continues to raise questions in and beyond experimental cellular immunology. Its structure as a 7 transmembrane G Protein-Coupled Receptor initiated the discovery of a diverse family of plasma membrane receptors. This review will trace milestones of research into the expression of F4/80, also known as Emr1, its value as a marker in formulation of the Mononuclear Phagocyte System and its function in a model of peripheral immune tolerance in the anterior chamber of the eye. Human EMR1 is closely related to a primate-restricted myeloid mechanoreceptor, EMR2, with a novel autocatalytic activation mechanism. We describe their relation to structurally related members of the group E adhesion GPCR subfamily and their contributions to homeostatic systems of the body through local plasma membrane cellular interactions.

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来源期刊
Journal of Leukocyte Biology
Journal of Leukocyte Biology 医学-免疫学
CiteScore
11.50
自引率
0.00%
发文量
358
审稿时长
2 months
期刊介绍: JLB is a peer-reviewed, academic journal published by the Society for Leukocyte Biology for its members and the community of immunobiologists. The journal publishes papers devoted to the exploration of the cellular and molecular biology of granulocytes, mononuclear phagocytes, lymphocytes, NK cells, and other cells involved in host physiology and defense/resistance against disease. Since all cells in the body can directly or indirectly contribute to the maintenance of the integrity of the organism and restoration of homeostasis through repair, JLB also considers articles involving epithelial, endothelial, fibroblastic, neural, and other somatic cell types participating in host defense. Studies covering pathophysiology, cell development, differentiation and trafficking; fundamental, translational and clinical immunology, inflammation, extracellular mediators and effector molecules; receptors, signal transduction and genes are considered relevant. Research articles and reviews that provide a novel understanding in any of these fields are given priority as well as technical advances related to leukocyte research methods.
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